Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_provenance.
- NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_assertion description "[We conclude that central cerebral white matter affection, spinal atrophy, and extrapyramidal symptoms are more often present in patients with pronounced deficiency of the GH/IGF-1 axis accompanied by markedly reduced body weight and high ataxia scores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_provenance.
- NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_assertion evidence source_evidence_literature NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_provenance.
- NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_assertion SIO_000772 19898915 NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_provenance.
- NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_assertion wasDerivedFrom befree-20150227 NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_provenance.
- NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_assertion wasGeneratedBy ECO_0000203 NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP424148.RAcAEGhVo9N4MgIKnCMo-Ugz6H_LuAHs8PFw8b9KIGqkc130_provenance.